Practical considerations to guide development of access controls and decision support for genetic information in electronic medical records (Q34065138)

30 July 2017

title

Practical considerations to guide development of access controls and decision support for genetic information in electronic medical records (English)

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30 July 2017

main subject

decision support system

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Diana C Darcy

1

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30 July 2017

Eleanor T Lewis

2

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30 July 2017

Kelly E Ormond

3

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30 July 2017

David J Clark

4

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30 July 2017

Jodie A Trafton

5

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30 July 2017

publication date

2 November 2011

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BMC Health Services Research

30 July 2017

published in

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30 July 2017

volume

11

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30 July 2017

page(s)

294

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Identification and Management of Women With BRCA Mutations or Hereditary Predisposition for Breast and Ovarian Cancer

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Pharmacogenomics: will the promise be fulfilled?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Exclusion of genetic information from the medical record: ethical and medical dilemmas

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Genomic electronic health records: opportunities and challenges

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

The futility of genomic counseling: essential role of electronic health records

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Delivery of genomic medicine for common chronic adult diseases: a systematic review

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Associations between anticipated reactions to genetic test results and interest in genetic testing: will self-selection reduce the potential for harm?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Patients' and healthcare professionals' views on pharmacogenetic testing and its future delivery in the NHS.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Status of clinical gene sequencing data reporting and associated risks for information loss

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

The genome-enabled electronic medical record

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Family history: a comprehensive genetic risk assessment method for the chronic conditions of adulthood

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Are electronic health records ready for genomic medicine?

5 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Confidentiality, privacy, and security of genetic and genomic test information in electronic health records: points to consider

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Pharmacogenetics of coumarinic oral anticoagulants

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

An agenda for personalized medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Concordance study of 3 direct-to-consumer genetic-testing services

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Evaluation of risk prediction updates from commercial genome-wide scans

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Key Internet genetics resources for the clinician

21 January 2018

1 reference

12 December 2020

Genetic information: Special or not? Responses from focus groups with members of a health maintenance organization

1 reference

12 December 2020

Ensuring security of high-risk information in EHRs

1 reference

12 December 2020

Keeping Pace with the Times — The Genetic Information Nondiscrimination Act of 2008

1 reference

12 December 2020

Family physicians' awareness and knowledge of the Genetic Information Non-Discrimination Act (GINA)

1 reference

12 December 2020

Genetic exceptionalism. Too much of a good thing?

1 reference

12 December 2020

Genetic exceptionalism & legislative pragmatism

1 reference

12 December 2020

Identifiers

DOI

10.1186/1472-6963-11-294

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Dimensions Publication ID

30 July 2017

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30 July 2017

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